Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.09.18.752591

Epidemic size and host-parasite (co)-evolution: a meta-analysis

Abstract

The size of an epidemic can influence the strength of selection acting on hosts and parasites, but whether epidemic size consistently shapes host-parasite (co)-evolution remains unclear. I conducted a meta-analysis of studies that simultaneously quantified epidemic size and evolutionary change in hosts, parasites or their interactions, synthesising 123 effect sizes from 11 studies. I tested whether epidemic size was associated with four components of evolutionary change: host evolution, parasite evolution, non-additive host-parasite coevolution and net coevolution. Larger epidemics were associated with greater host evolutionary change in invertebrates, whereas the relationship was positive in plants and negative but non-significant in bacteria. Parasite evolution, non-additive coevolution and net coevolution were not detectably associated with epidemic size, although parasite infectivity showed a relatively consistent increase across studies. These results provide limited evidence for a general relationship between epidemic size and host-parasite (co)-evolution and instead suggest that evolutionary responses depend on the host-parasite system and broader ecological and temporal context. Interpretation is constrained by the small and taxonomically biased evidence base, particularly the strong representation of Daphnia, and by substantial heterogeneity in how epidemic size and evolutionary change were measured and defined. More studies across diverse host-parasite systems are required that track both evolutionary change and disease prevalence through time. This work also provides an empirical basis for incorporating coevolutionary feedbacks into quantitative epidemiological models.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Paplauskas, S.. 2026-09-18. Epidemic size and host-parasite (co)-evolution: a meta-analysis. https://doi.org/10.64898/2026.09.18.752591

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

RELAX does not reproduce its own estimates at default settings, and its output does not show it

Selection-intensity estimates from RELAX are reported as a point value of K with a likelihood-ratio P. We report that, at default settings and on data of ordinary size, the program does not reproduce its own fits. Of 27 enzyme entries refitted under two optimiser configurations, none reproduced its log-likelihood to within 0.01 units; the median change was 103 units, the largest over 3,400, and four verdicts reversed. Eighty null orthologues reproduced none. A byte-identical command returned a distinct likelihood on every repetition, single-threaded, across three releases, and on alignments simulated under the fitted model, where 3.3 per cent of replicates reproduced. The documented random-number seed never reaches the generator when assigned on the command line, yet reads back as the value supplied. PAML localises the cause: its two-ratio model, without site classes, reproduced its log-likelihood for all 288 genes; its site-class models agreed for 27 to 67 per cent. The instability follows the mixture over sites, not the program. The output does not show it: 46 of 410 fits ended with a negative likelihood-ratio statistic, impossible under convergence, and 123 of 410 report a K re-estimated under a domain restriction rather than the unconstrained maximum. Of 234 published studies using RELAX, none reported a seed. Seeding while holding the thread count at one reproduced sixty of sixty runs on twenty genes under two releases; the seed alone reproduced none of five, and no documentation states the second condition. We recommend that fits be repeated and their dispersion published.

evolutionary biology↗

Sequential accumulation of adaptive alleles forms an inversion supergene in deer mice

Supergenes are clusters of co-inherited loci that affect multiple or complex phenotypes. Despite the growing number of chromosomal inversions identified as supergenes in natural populations, their molecular basis and evolutionary history often remain obscure. Here, we identified two candidate genes, Slc45a2 and Npr3, within a 41-Mb inversion supergene in the deer mouse (Peromyscus maniculatus) that respectively drive darker coats and longer tails - two traits associated with forest adaptation. Mice homozygous for the inversion (inv/inv) exhibit elevated Slc45a2 expression in melanocytes relative to the congenic standard genotype (std/std), disrupting pheomelanin production. In parallel, downregulation of Npr3 in inv/inv mouse growth plates prolongs postnatal growth of caudal vertebrae, resulting in tail elongation. Population-level analyses further implicate that this supergene arose through the subsequent accumulation of the Npr3 allele within the inversion, rather than by capturing all beneficial mutations at its origin.

evolutionary biology↗

Toxin structure shapes palatability in a chemically defended butterfly

The toxicity of chemical defences is well studied, but the potential contribution of compound structure to predator deterrence remains largely unexplored. Whether predation acts more strongly on toxicity or unpalatability remains largely untested, partly because few systems allow toxin structure to vary independently of quantity. Heliconius sara larvae provide such a system: those reared on Passiflora auriculata sequester cyclopentenyl cyanogenic glucosides (CGs), while those reared on P. biflora biosynthesise comparable quantities of aliphatic CGs. Using two invertebrate predators, Camponotus floridanus ants and Hierodula membranacea mantids, we tested whether this structural difference affects palatability independent of toxicity. Mantids rejected larvae with cyclopentenyl CGs more often than larvae with aliphatic CGs, despite no detectable difference in total CG content. This pattern was mirrored in extract-based assays with ants, independently of cyanide release: extracts with cyclopentenyl CGs remained deterrent, while extracts with aliphatic CGs did not differ in deterrence from water. Live larvae, by contrast, elicited similar responses from ants regardless of CG structure. These results show that variation in toxin structure can strongly affect palatability, with some compounds conferring greater protection than others. This demonstrates the importance of chemical structural diversity in the evolution of chemical defences.

evolutionary biology↗